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01 1AbbVie Inc. North Chicago US
02 1SM BIOMED SDN BHD Sungai Petani MY
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01 2Erythromycin stearate
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01 1Malaysia
02 1U.S.A
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01 1Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 1999-120 - Rev 03
Status : Valid
Issue Date : 2023-03-08
Type : Chemical
Substance Number : 490
Certificate Number : R1-CEP 2002-233 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2013-01-30
Type : Chemical and TSE
Substance Number : 490
87
PharmaCompass offers a list of Erythromycin Stearate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Erythromycin Stearate manufacturer or Erythromycin Stearate supplier for your needs.
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A Erythromycin stearate [BAN:JAN] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Erythromycin stearate [BAN:JAN], including repackagers and relabelers. The FDA regulates Erythromycin stearate [BAN:JAN] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Erythromycin stearate [BAN:JAN] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Erythromycin stearate [BAN:JAN] supplier is an individual or a company that provides Erythromycin stearate [BAN:JAN] active pharmaceutical ingredient (API) or Erythromycin stearate [BAN:JAN] finished formulations upon request. The Erythromycin stearate [BAN:JAN] suppliers may include Erythromycin stearate [BAN:JAN] API manufacturers, exporters, distributors and traders.
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A Erythromycin stearate [BAN:JAN] CEP of the European Pharmacopoeia monograph is often referred to as a Erythromycin stearate [BAN:JAN] Certificate of Suitability (COS). The purpose of a Erythromycin stearate [BAN:JAN] CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Erythromycin stearate [BAN:JAN] EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Erythromycin stearate [BAN:JAN] to their clients by showing that a Erythromycin stearate [BAN:JAN] CEP has been issued for it. The manufacturer submits a Erythromycin stearate [BAN:JAN] CEP (COS) as part of the market authorization procedure, and it takes on the role of a Erythromycin stearate [BAN:JAN] CEP holder for the record. Additionally, the data presented in the Erythromycin stearate [BAN:JAN] CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Erythromycin stearate [BAN:JAN] DMF.
A Erythromycin stearate [BAN:JAN] CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Erythromycin stearate [BAN:JAN] CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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